Wei E. I. Sha

Dual Plasmonic Nanostructures for High Performance Inverted Organic Solar Cells

Polymer-fullerene-based bulk heterojunction (BHJ) solar cells have many advantages, including low-cost, low-temperature fabrication, semi-transparency, and mechanical fl exibility. [ 1 , 2 ] However, there is a mismatch between optical absorption length and charge transport scale. [ 3 , 4 ] These factors lead to recombination losses, higher series resistances, and lower fi ll factors. Attempts to optimize both the optical and electrical properties of the photoactive layer in organic solar cells (OSCs) inevitably result in a demand to develop a device architecture that can enable effi cient optical absorption in fi lms thinner than the optical absorption length. [ 5 , 6 ] Here, we report the use of two metallic nanostructures to achieve broad light absorption enhancement, increased shortcircuit current ( J sc ), and improved fi ll factor ( FF ) simultaneously based on the new small-bandgap polymer donor poly{[4,8-bis(2-ethyl-hexyl-thiophene-5-yl)-benzo[1,2-b:4,5-b ′ ]dithiophene2,6-diyl]alt -[2-(2 ′ -ethyl-hexanoyl)-thieno[3,4-b]thiophen-4,6-diyl]} (PBDTTT-C-T) in BHJ cells. [ 7 ] The dual metallic nanostructure consists of a metallic nanograting electrode as the back refl ector and metallic nanoparticles (NPs) embedded in the active layer. Consequently, we achieve the high power conversion effi ciency (PCE) of 8.79% for a single-junction BHJ OSC. Recently, plasmonic nanostructures have been introduced into solar cells for highly effi cient light harvesting. [ 5 , 8–17 ] Two types of plasmonic resonances, surface plasmonic resonances (SPRs) [ 18–22 ] and localized plasmonic resonances (LPRs), [ 11–14 ] can be used for enhancing light absorption. Metallic gratingbased light-trapping schemes have been investigated in traditional inorganic photovoltaic cells. [ 18–20 ] For metallic nanogratings, which can support SPRs, it is still challenging to experimentally demonstrate the enhancement of PCE in OSCs owing to the obvious issue of solution processing of

Optical and electrical properties of efficiency enhanced polymer solar cells with Au nanoparticles in a PEDOT–PSS layer

We unveil new device physics and provide details of device mechanisms by investigating polymer solar cells (PSCs) incorporating Au nanoparticles (NPs) into the hole collection poly(3,4-ethylenedioxythiophene) poly(styrenesulfonate) (PEDOT:PSS) layer. Theoretical and experimental results show that the very strong near field around Au NPs due to Localized Surface Plasmonic Resonance (LSPR) mainly distributes laterally along the PEDOT:PSS layer rather than vertically into the adjacent active layer, leading to minimal enhancement of light absorption in the active layer. This finding can be extended to a typical class of solar cells incorporating metallic NPs in spacing layers adjacent to the active layer. With optical effects proven to be minor contributors to device performance improvements, we investigate the electrical properties of the PSCs and obtain insights into the detailed device mechanisms. Improvements in power conversion efficiency (PCE) of solar cells are found to originate from the enlarged active layer/PEDOT:PSS interfacial area and improved PEDOT:PSS conductivity. At high NP concentrations, reduced exciton quenching at donor/acceptor junctions is found to cause PCE deterioration. Our findings indicate that it is highly important to investigate both optical and electrical effects for understanding and optimizing PSC performances.

Optical and electrical effects of gold nanoparticles in the active layer of polymer solar cells

The effects of Au nanoparticles (NPs) incorporated into the active layer of polymer solar cells (PSCs) with a newly synthesized donor polymer are investigated in detail. Our work shows that localized surface plasmon resonance (LSPR) introduced by the metallic NPs can experimentally and theoretically enhance the light absorption in the active layer of PSCs because the strong LSPR near field mainly distributes laterally along the active layer. The understanding can be applied to other metallic NP incorporated organic solar cells. Meanwhile, our results show that electrical properties can counter-diminish the optical enhancement from LSPR and thus reduce the overall performance improvement. It is important that both optical and electrical properties need to be studied and optimized simultaneously for achieving improved power conversion efficiency. The study contributes to better understanding the uses of Au NPs for enhancing PSC performances.

The efficiency limit of CH3NH3PbI3 perovskite solar cells

With the consideration of photon recycling effect, the efficiency limit of methylammonium lead iodide (CH3NH3PbI3) perovskite solar cells is predicted by a detailed balance model. To obtain convincing predictions, both AM 1.5 spectrum of Sun and experimentally measured complex refractive index of perovskite material are employed in the detailed balance model. The roles of light trapping and angular restriction in improving the maximal output power of thin-film perovskite solar cells are also clarified. The efficiency limit of perovskite cells (without the angular restriction) is about 31%, which approaches to Shockley-Queisser limit (33%) achievable by gallium arsenide (GaAs) cells. Moreover, the Shockley-Queisser limit could be reached with a 200 nm-thick perovskite solar cell, through integrating a wavelength-dependent angular-restriction design with a textured light-trapping structure. Additionally, the influence of the trap-assisted nonradiative recombination on the device efficiency is investigated. The work is fundamentally important to high-performance perovskite photovoltaics.

Improving the efficiency of polymer solar cells by incorporating gold nanoparticles into all polymer layers

We demonstrate efficiency improvement in polymer solar cells (PSCs) by ∼22% through incorporating Au nanoparticles (NPs) into all polymer layers. Au NPs are found to have distinct mechanisms in improving device performance when incorporated in different polymer layers. Au NPs in poly‐(3,4‐ethylenedioxythiophene):poly(styrenesulfonate) mainly contribute to better hole collection while Au NPs in active layer contributes to the enhanced optical absorption and more balanced charge‐transport. Our theoretical result shows that the absorption enhancement at the active layer is attributed to plasmon resonances with strong near‐field distributions penetrated into absorption polymers. These findings can be applied to design high‐efficiency metallic NPs‐incorporated PSCs.

Near-field multiple scattering effects of plasmonic nanospheres embedded into thin-film organic solar cells

We investigate near-field multiple scattering effects of plasmonic nanospheres (NSPs) embedded into organic solar cells (OSCs). When NSPs are embedded into a spacer layer, the near-field scattering from the NSPs shows strong direction-dependent features, which significantly affects the optical absorption. When NSPs are embedded into an active layer, the absorption enhancement is attributed to the interplay between longitudinal and transverse modes supported by the NSP chain. The breakdown of electrostatic scaling law is confirmed by our theoretical model and should be accounted for optical designs of OSCs. The work provides the fundamental physical understanding and design guidelines for plasmonic photovoltaics.

Photocatalytic decomposition of 4-t-octylphenol over NaBiO3 driven by visible light: Catalytic kinetics and corrosion products characterization

The photocatalytic decomposition of 4-t-octylphenol (4-t-OP) by NaBiO(3) photocatalyst and the catalyst stability in aqueous solution were investigated systematically for the first time. The results showed that some parameters such as catalyst dosage, initial 4-t-OP concentration and pH value of the solution had great effects on the photocatalytic activity. The NaBiO(3) photocatalyst maintained considerable catalytic performance under visible light (lambda>400 nm) irradiation and exhibited a higher photocatalytic activity compared to the commercialized photocatalyst P25. In addition, the corrosion products of NaBiO(3) catalyst under acid condition (HCl aqueous solution contained) were characterized by X-ray diffraction (XRD), transmittance electronic microscopy (TEM), selected area electron diffraction (SAED), X-ray photoelectron spectroscopy (XPS) and UV-vis transmittance spectrum analysis. The results showed that NaBiO(3) was unstable under the acidic condition and the catalyst could convert into Bi(3+)-containing compounds such as Bi(2)O(3), etc. The experiment demonstrates that NaBiO(3) can be corroded to nano-sized BiOCl crystal in the presence of hydrogen chloride, the band gap of which was estimated to be 3.28 eV by Taucs approach.

Angular response of thin-film organic solar cells with periodic metal back nanostrips

We theoretically study the angular response of thin-film organic solar cells with periodic Au back nanostrips. In particular, the equation of the generalized Lamberts cosine law for arbitrary periodic nanostructure is formulated. We show that the periodic strip structure achieves wide-angle absorption enhancement compared with the planar nonstrip structure for both the s- and p-polarized light, which is mainly attributed to the resonant Woods anomalies and surface plasmon resonances, respectively. The work is important for designing and optimizing high-efficiency photovoltaic cells.

A comprehensive study for the plasmonic thin-film solar cell with periodic structure

A comprehensive study of the plasmonic thin-film solar cell with the periodic strip structure is presented in this paper. The finite-difference frequency-domain method is employed to discretize the inhomogeneous wave function for modeling the solar cell. In particular, the hybrid absorbing boundary condition and the one-sided difference scheme are adopted. The parameter extraction methods for the zeroth-order reflectance and the absorbed power density are also discussed, which is important for testing and optimizing the solar cell design. For the numerical results, the physics of the absorption peaks of the amorphous silicon thin-film solar cell are explained by electromagnetic theory; these peaks correspond to the waveguide mode, Floquet mode, surface plasmon resonance, and the constructively interference between adjacent metal strips. The work is therefore important for the theoretical study and optimized design of the plasmonic thin-film solar cell.

Optical and electrical study of organic solar cells with a 2D grating anode

We investigate both optical and electrical properties of organic solar cells (OSCs) incorporating 2D periodic metallic back grating as an anode. Using a unified finite-difference approach, the multiphysics modeling framework for plasmonic OSCs is established to seamlessly connect the photon absorption with carrier transport and collection by solving the Maxwells equations and semiconductor equations (Poisson, continuity, and drift-diffusion equations). Due to the excited surface plasmon resonance, the significantly nonuniform and extremely high exciton generation rate near the metallic grating are strongly confirmed by our theoretical model. Remarkably, the nonuniform exciton generation indeed does not induce more recombination loss or smaller open-circuit voltage compared to 1D multilayer standard OSC device. The increased open-circuit voltage and reduced recombination loss by the plasmonic OSC are attributed to direct hole collections at the metallic grating anode with a short transport path. The work provides an important multiphysics understanding for plasmonic organic photovoltaics.